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Starting soon Phase 2

A Study to Evaluate Efficacy and Safety of BGM1812 Injection in Overweight or Obese Participants Without Diabetes

NCT07918625 · tracked via the Priya Life Science China tracker
Phase
Phase 2
Started
2026-11-30
Last updated
2026-11-05

Condition(s) studied

Overweight or Obese Participants Without Diabetes

Investigational drug(s) / intervention(s)

BGM1812 injection / plcaeboBGM1812 injection / plcaeboBGM1812 injection / plcaeboBGM1812 injection / plcaebo

BGM1812 injection / plcaebo: Once weekly or once every two weeks, administered continuously for 24 weeks.

BGM1812 injection / plcaebo: Once weekly or once every two weeks, administered continuously for 24 weeks.

BGM1812 injection / plcaebo: Once weekly or once every two weeks, administered continuously for 24 weeks.

BGM1812 injection / plcaebo: Once weekly or once every two weeks, administered continuously for 24 weeks.

Study summary

To evaluate the efficacy of BGM1812 injection compared with placebo in reducing body weight in overweight or obese participants without diabetes after 26 weeks of treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * ○ Participants must be Chinese, non-diabetic, overweight or obese individuals aged 18 to 55 years (inclusive), as determined by the time of signing the informed consent form. Both men and women are eligible. * Obese participants: BMI ≥ 28.0 kg/m²; or overweight participants: 24.0 kg/m² ≤ BMI \< 28.0 kg/m² and have at least one of the following conditions: i. Pre-diabetes (impaired fasting glucose and/or impaired glucose tolerance), hypertension, non-alcoholic fatty liver disease, or dyslipidemia; ii. Weight-bearing joint pain; iii. Obesity-induced breathing difficulties or obstructive sleep apnea syndrome. * Participants must have undergone at least 12 weeks of diet and exercise control before screening, with a weight change of less than 5.0% (self-reported), and be willing to continue with the same diet and exercise control during the trial period. Exclusion Criteria: * ● Within the previous 12 weeks, used drugs for weight control. * Within the previous 12 weeks, used other drugs or supplements for weight loss purposes, or meal replacement products, including other prescription drugs, over-the-counter drugs, Chinese herbal medicines, supplements, meal replacement products (whether for weight loss purposes is determined by the prescription or product instructions). * At the screening/baseline stage, any one of the following laboratory test indicators meets the following criteria: Glycated hemoglobin (HbA1c) ≥6.5%, fasting blood glucose ≥7.0 mmol/L, or 2-hour blood glucose of oral glucose tolerance test (OGTT) ≥11.1 mmol/L (during screening, participants with fasting blood glucose ranging from 6.1 to 6.9 mmol/L need to undergo the OGTT test). * There is a history or evidence of any of the following diseases:1) (Interview) It belongs to a secondary disease or drug-induced obesity, including: elevated cortisol hormone (such as Cushing's syndrome), obesity caused by damage to the pituitary and hypothalamus, obesity caused by reducing or discontinuing weight loss drugs, etc.;2) (Interview/Examination) Previously or during screening diagnosed with type 1 or type 2 diabetes;3) (Interview) Previously diagnosed with acute or chronic pancreatitis, or pancreatic injury;4) (Interview) Previously diagnosed with thyroid C-cell carcinoma, MEN (multiple endocrine neoplasia) type 2A or 2B, or having a related family history. * Previously had a moderate or severe depression history, or during screening the PHQ-9 (depression screening scale) questionnaire was ≥ 15 points, or had a history of other serious mental illness, or had suicidal tendencies or suicidal behavior.

Primary outcome measure(s)

  • Percent Change from Baseline in Body Weight — 24 weeks
    Percentage change in fasting body weight from baseline after 24 weeks of treatment

Trial sites (1)

FacilityCityRegionStatus
The Second Affiliated Hospital of Soochow University Changsha Hunan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07918625 on ClinicalTrials.gov ↗ ← All trials in China